About: (2R,3R)-1,4-Dimethoxy-1,1,4,4-tetraphenyl-2,3-butanediol: Chiral Auxiliary and Efficient Protecting Group for Boronic Acids

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About: (2R,3R)-1,4-Dimethoxy-1,1,4,4-tetraphenyl-2,3-butanediol: Chiral Auxiliary and Efficient Protecting Group for Boronic Acids Goto Sponge NotDistinct Permalink

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scientific article published on 01 December 2000

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в грудні 2000 (uk) مقالة علمية تنشرت ف 1 دجنبر 2000 (ary) article scientifique publié en 2000 (fr) im Dezember 2000 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu n'avientu de 2000 (ast) scientific article published on 01 December 2000 (en)
publication date	wds:Q58072350-AD820946-803F-4C97-A8C9-45139FBA70A0
publication date	2000-12-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q58072350-9BC522EF-0969-4F73-B58D-9289B2995E51
language of work or name	English
cites work	wds:Q58072350-8E0B7E85-C482-497E-8EC4-D117987E4A55
cites work	(Chloromethyl)lithium: efficient generation and capture by boronic esters and a simple preparation of diisopropyl (chloromethyl)boronate
author name string	wds:Q58072350-87368335-852B-455F-A3A1-5BC954AC297D
author name string	Luithle JE
rdfs:label	(2R,3R)-1,4-Dimethoxy-1,1,4,4-tetraphenyl-2,3-butanediol: Chiral Auxiliary and Efficient Protecting Group for Boronic Acids (en) (2R,3R)-1,4-Dimethoxy-1,1,4,4-tetraphenyl-2,3-butanediol: Chiral Auxiliary and Efficient Protecting Group for Boronic Acids (nl)
skos:prefLabel	(2R,3R)-1,4-Dimethoxy-1,1,4,4-tetraphenyl-2,3-butanediol: Chiral Auxiliary and Efficient Protecting Group for Boronic Acids (en) (2R,3R)-1,4-Dimethoxy-1,1,4,4-tetraphenyl-2,3-butanediol: Chiral Auxiliary and Efficient Protecting Group for Boronic Acids (nl)
name	(2R,3R)-1,4-Dimethoxy-1,1,4,4-tetraphenyl-2,3-butanediol: Chiral Auxiliary and Efficient Protecting Group for Boronic Acids (en) (2R,3R)-1,4-Dimethoxy-1,1,4,4-tetraphenyl-2,3-butanediol: Chiral Auxiliary and Efficient Protecting Group for Boronic Acids (nl)
author	wds:Q58072350-8940918E-7373-487C-8C39-5B7D8724479B
author	Jörg Pietruszka
title	wds:Q58072350-1BA56A8D-E025-4028-9B2F-F06C8D3BF948
title	(2R,3R)-1,4-Dimethoxy-1,1,4,4-tetraphenyl-2,3-butanediol: chiral auxiliary and efficient protecting group for boronic acids (en)
page(s)	wds:Q58072350-A07D0F4E-A3F6-4C34-BF41-FF602BF02908
page(s)	9194-9200
instance of	wds:Q58072350-FC87121A-D0E6-459E-9FFD-505A7FC906A4
instance of	scholarly article
main subject	wds:Q58072350-36745D18-B416-4629-9D0E-D2C97F488B2A wds:Q58072350-CDE7B7E2-B2F0-4433-959B-5F032C04A66A
main subject	chirality boronic acid
PubMed ID	wds:Q58072350-21421CD8-84BD-41C5-AD29-9B4E833F981F
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/11149869
PubMed ID	11149869
published in	wds:Q58072350-5DEAFEA4-0C0D-44A8-849E-DE50E5DB5677
published in	Journal of Organic Chemistry
issue	wds:Q58072350-1781505F-A65B-4881-B065-5E5A5E1A6A8A
volume	wds:Q58072350-684FF14E-6015-492B-8E66-AB67F84B81C7
issue	26
volume	65
DOI	wds:Q58072350-A5CF602E-C9AE-4007-A725-CDF9474FD1E4
DOI	http://dx.doi.org/10.1021/JO0056601
DOI	10.1021/JO0056601
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q58072350
is cites work of	Chemical behaviour of a prototype boryl(phosphino)carbene Enantiomerically Pure Vinylcyclopropylboronic Esters Multistep synthesis of complex boronic acids from simple MIDA boronates Iterative Cross-Couplng with MIDA Boronates: Towards a General Platform for Small Molecule Synthesis Enantiomerically Pure Cyclopropylamines from Cyclopropylboronic Esters Synthesis of enantiomerically pure vinylcyclopropylboronic esters via cross-metathesis Enantioselective and Enantiospecific Transition-Metal-Catalyzed Cross-Coupling Reactions of Organometallic Reagents To Construct C-C Bonds Configurationally Stable, Enantioenriched Organometallic Nucleophiles in Stereospecific Pd-Catalyzed Cross-Coupling Reactions: An Alternative Approach to Asymmetric Synthesis Development of Enantiospecific Coupling of Secondary and Tertiary Boronic Esters with Aromatic Compounds Synthesis of Alkenylboronic Esters: An Alternative Route to Trisubstituted Homoallylic Alcohols Diasteroselective preparation of cyclopropanols using methylene bis(iodozinc). Enantio- and Diastereoselective Cyclopropanation of 1-Alkenylboronates: Synthesis of 1-Boryl-2,3-Disubstituted Cyclopropanes.
is cites work of	wds:Q30703255-14501C28-7307-4ACE-ADF9-ACCAC65758D8 wds:Q41910817-CE25BE5E-6B29-4C73-9820-3637D24F5DA8 wds:Q58071706-F6F0EC67-8EF1-4363-83D2-FB730E9C68B7 wds:Q41456345-355B931B-BFD0-43F4-9B57-1E834A98D88B wds:Q46329999-66402035-A932-4411-9F95-14FA5D332E01 wds:Q36049587-ED6CA532-023D-4915-8673-88499D385578 wds:Q34494948-3AE85095-0CDC-41D1-82D2-B96CA5BE580E wds:Q34890091-54CD5E36-2F95-4BA1-82C0-C1EE306B3DE2 wds:Q48143914-E3819F8B-76B7-4594-9049-F380DF2E47D3 wds:Q58072192-4F0A11B8-1088-4916-9789-D1295D3B98B9 wds:Q58072328-E9471D65-CC3C-45B9-8EE0-5169C2E923E0 wds:Q58072199-B5C839CC-1307-4FD8-A6A1-B532C73BB5B9

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